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Author: Jaana Suvisaari

  • Most recently observed institution: National Institute for Health and Welfare, Helsinki, Finland

Rankings

  • All-time downloads: 8,994 (rank: 9,157 (tie) out of 383,004)
  • Categories:
    • genetics: 6,086 (rank: 2,801 (tie) out of 35,377)
    • genomics: 2,823 (rank: 6,848 (tie) out of 40,806)
    • neuroscience: 85 (rank: 62,620 (tie) out of 64,259)

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Preprints

Ultra-rare disruptive and damaging mutations influence educational attainment in the general population

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A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

genomics more details view paper
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Rare loss-of-function variants in KMT2F are associated with schizophrenia and developmental disorders

genomics more details view paper
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Rare schizophrenia risk variants are enriched in genes shared with neurodevelopmental disorders

genetics more details view paper
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Contribution of rare and common variants to intellectual disability in a high-risk population sub-isolate of Northern Finland

genetics more details view paper
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Advantages of genotype imputation with ethnically matched reference panel for rare variant association analyses

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The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484

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Variants in regulatory elements of PDE4D associate with Major Mental Illness in the Finnish population

genetics more details view paper
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Molecular signaling pathways underlying schizophrenia

neuroscience more details view paper
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    • In neuroscience: 15,095 out of 15,898
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